Canonical Allele Identifier: CA2633898274

Gene: CDH1

Linked Data

• gnomAD v4: 16-68808483-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808485_68808486del , CM000678.2:g.68808485_68808486del	GRCh38
NC_000016.9:g.68842388_68842389del , CM000678.1:g.68842388_68842389del	GRCh37
NC_000016.8:g.67399889_67399890del	NCBI36
NG_008021.1:g.76194_76195del , LRG_301:g.76194_76195del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.449_450del MANE Select	ENSP00000261769.4:p.Arg150LysfsTer17
ENST00000261769.9:c.449_450del	ENSP00000261769.4:p.Arg150LysfsTer17
ENST00000422392.6:c.449_450del	ENSP00000414946.2:p.Arg150LysfsTer17
ENST00000561751.1:c.216_217del
ENST00000562836.5:n.520_521del
ENST00000564676.5:n.731_732del
ENST00000564745.1:n.444_445del
ENST00000566510.5:c.449_450del	ENSP00000458139.1:p.Arg150LysfsTer17
ENST00000566612.5:c.449_450del	ENSP00000454782.1:p.Arg150LysfsTer17
ENST00000611625.4:c.449_450del	ENSP00000481063.1:p.Arg150LysfsTer17
ENST00000612417.4:c.449_450del	ENSP00000478360.1:p.Arg150LysfsTer17
ENST00000621016.4:c.449_450del	ENSP00000480664.1:p.Arg150LysfsTer17
NM_004360.3:c.449_450del , LRG_301t1:c.449_450del	NP_004351.1:p.Arg150LysfsTer17
XM_011523488.1:c.-287_-286del	XP_011521790.1:n.-287_-286del
XM_011523489.1:c.-287_-286del	XP_011521791.1:n.-287_-286del
NM_001317184.1:c.449_450del	NP_001304113.1:p.Arg150LysfsTer17
NM_001317185.1:c.-1167_-1166del	NP_001304114.1:n.-1167_-1166del
NM_001317186.1:c.-1371_-1370del	NP_001304115.1:n.-1371_-1370del
NM_004360.4:c.449_450del	NP_004351.1:p.Arg150LysfsTer17
NM_004360.5:c.449_450del MANE Select	NP_004351.1:p.Arg150LysfsTer17
NM_001317184.2:c.449_450del	NP_001304113.1:p.Arg150LysfsTer17
NM_001317185.2:c.-1167_-1166del	NP_001304114.1:n.-1167_-1166del
NM_001317186.2:c.-1371_-1370del	NP_001304115.1:n.-1371_-1370del